{"title":"[整合酶和逆转录酶:对艾滋病毒基因组复制系统的新认识]","authors":"Takao Masuda, Gota Kawai","doi":"10.2222/jsv.73.139","DOIUrl":null,"url":null,"abstract":"<p><p>Reverse transcriptase (RT) and integrase (IN) are retrovirus enzymes to convert virus genomic RNA into provirus DNA state in host cells. The RT and IN encoded tandemly in the pol gene, are translated as a fused form and incorporated into the virus particles. Recently, we discovered the potential role of HIV-1 IN to regulate the reverse transcription through the fused state with RT (RT-IN). On the other hand, analysis of HIV-1 transcripts have revealed the variations in number of guanine residue at the 5' end (5'G) due to fluctuations in the transcription initiation point within HIV-1 provirus DNA. Importantly, the number of 5'G dictates the packaging of HIV genome RNA into virus particles serving as a template for the reverse transcription reaction. In this review, we provide new insights into the mechanism of HIV genome replication based on our recent findings of the structural-functional correlation of HIV enzymes (RT and IN) and virus genomic RNA.</p>","PeriodicalId":75275,"journal":{"name":"Uirusu","volume":"73 2","pages":"139-146"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Integrase and reversetranscriptase: New insights into the HIV genome replication system in line.]\",\"authors\":\"Takao Masuda, Gota Kawai\",\"doi\":\"10.2222/jsv.73.139\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Reverse transcriptase (RT) and integrase (IN) are retrovirus enzymes to convert virus genomic RNA into provirus DNA state in host cells. The RT and IN encoded tandemly in the pol gene, are translated as a fused form and incorporated into the virus particles. Recently, we discovered the potential role of HIV-1 IN to regulate the reverse transcription through the fused state with RT (RT-IN). On the other hand, analysis of HIV-1 transcripts have revealed the variations in number of guanine residue at the 5' end (5'G) due to fluctuations in the transcription initiation point within HIV-1 provirus DNA. Importantly, the number of 5'G dictates the packaging of HIV genome RNA into virus particles serving as a template for the reverse transcription reaction. In this review, we provide new insights into the mechanism of HIV genome replication based on our recent findings of the structural-functional correlation of HIV enzymes (RT and IN) and virus genomic RNA.</p>\",\"PeriodicalId\":75275,\"journal\":{\"name\":\"Uirusu\",\"volume\":\"73 2\",\"pages\":\"139-146\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Uirusu\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2222/jsv.73.139\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Uirusu","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2222/jsv.73.139","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
逆转录酶(RT)和整合酶(IN)是逆转录病毒的酶,可将病毒基因组 RNA 转化为宿主细胞中的前病毒 DNA 状态。反转录酶和整合酶在 pol 基因中串联编码,以融合的形式翻译并整合到病毒颗粒中。最近,我们发现了 HIV-1 IN 通过与 RT 的融合状态(RT-IN)调节逆转录的潜在作用。另一方面,对 HIV-1 转录本的分析表明,由于 HIV-1 前病毒 DNA 中转录起始点的波动,5'端鸟嘌呤残基(5'G)的数量也会发生变化。重要的是,5'G 的数量决定了将 HIV 基因组 RNA 包装成病毒颗粒,作为反转录反应的模板。在这篇综述中,我们根据最近对 HIV 酶(RT 和 IN)与病毒基因组 RNA 的结构-功能相关性的研究结果,对 HIV 基因组复制的机制提出了新的见解。
[Integrase and reversetranscriptase: New insights into the HIV genome replication system in line.]
Reverse transcriptase (RT) and integrase (IN) are retrovirus enzymes to convert virus genomic RNA into provirus DNA state in host cells. The RT and IN encoded tandemly in the pol gene, are translated as a fused form and incorporated into the virus particles. Recently, we discovered the potential role of HIV-1 IN to regulate the reverse transcription through the fused state with RT (RT-IN). On the other hand, analysis of HIV-1 transcripts have revealed the variations in number of guanine residue at the 5' end (5'G) due to fluctuations in the transcription initiation point within HIV-1 provirus DNA. Importantly, the number of 5'G dictates the packaging of HIV genome RNA into virus particles serving as a template for the reverse transcription reaction. In this review, we provide new insights into the mechanism of HIV genome replication based on our recent findings of the structural-functional correlation of HIV enzymes (RT and IN) and virus genomic RNA.